ePRO Resources
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Training Program Reduces Placebo Effect By More Than 50% In ePRO Study
5/17/2023
Discover how an instruction program directly contributed to significantly lowering the placebo response rate in a phase III migraine CNS study.
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The Building Blocks Of DCT: How To Create A Seamless Experience Across eConsent, eCOA, And More
3/29/2022
With more than 76% of sponsors seeking to implement decentralized solutions this year, there’s never been more attention given to decentralized trials. Discover why decentralized trials must take a unified approach, one that alleviates burdens for patients and sites in order to drive cost savings and realize efficiencies.
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Addressing The Specific Complexities Of Oncology eCOA Clinical Trials
4/18/2022
What are the specific tools and keys to conduct eCOA trials in oncology successfully? This article identifies some of the relevant solutions to tackle oncology protocol complexities.
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Powering Your Research Potential: Elevating Participant Centric Research
4/19/2024
This flexible, web-based solution offers patient-centric experiences, ensuring efficient data capture and immediate insights. Transform how you gather and manage trial data for superior accuracy and participant engagement.
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Veeva eCOA Demo
6/24/2024
See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.
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Could ePRO Be The New Standard In Health Reimbursement?
1/30/2023
Recently, early-phase protocols have been collecting patient-reported outcomes (PROs) not only to get regulatory approval but to demonstrate value to public and private payers.
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Empowering Freenome: Large-Scale Data Quality And Compliance
10/17/2023
Delve into five ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.
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Modernizing Clinical Research With AI And Digital Data
3/7/2025
Discover how ActiGraph is revolutionizing clinical trials with patient-focused digital data and cutting-edge technology that enhances trial efficiency across all phases.
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Simplify Today. Transform For The Future.
10/25/2023
Maximize efficiency today with a cloud-based user-friendly platform that seamlessly adapts to the future of phase 1-3 trials. Watch to see how Zelta can help.
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Minimizing Hurdles For Patients During The eConsent Process
10/4/2022
Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.